Rozycka Aleksandra, Liguz-Lecznar Monika
Department of Molecular and Cellular Neurobiology, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur Street, Warsaw, 02-093, Poland.
Aging Cell. 2017 Aug;16(4):634-643. doi: 10.1111/acel.12605. Epub 2017 May 12.
As it was established that aging is not associated with massive neuronal loss, as was believed in the mid-20th Century, scientific interest has addressed the influence of aging on particular neuronal subpopulations and their synaptic contacts, which constitute the substrate for neural plasticity. Inhibitory neurons represent the most complex and diverse group of neurons, showing distinct molecular and physiological characteristics and possessing a compelling ability to control the physiology of neural circuits. This review focuses on the aging of GABAergic neurons and synapses. Understanding how aging affects synapses of particular neuronal subpopulations may help explain the heterogeneity of aging-related effects. We reviewed the literature concerning the effects of aging on the numbers of GABAergic neurons and synapses as well as aging-related alterations in their presynaptic and postsynaptic components. Finally, we discussed the influence of those changes on the plasticity of the GABAergic system, highlighting our results concerning aging in mouse somatosensory cortex and linking them to plasticity impairments and brain disorders. We posit that aging-induced impairments of the GABAergic system lead to an inhibitory/excitatory imbalance, thereby decreasing neuron's ability to respond with plastic changes to environmental and cellular challenges, leaving the brain more vulnerable to cognitive decline and damage by synaptopathic diseases.
正如人们所确定的那样,衰老并不像20世纪中叶所认为的那样与大量神经元丧失有关,科学兴趣已转向衰老对特定神经元亚群及其突触联系的影响,而这些构成了神经可塑性的基础。抑制性神经元是最复杂、最多样化的神经元群体,表现出独特的分子和生理特征,并具有控制神经回路生理功能的强大能力。本综述聚焦于γ-氨基丁酸能(GABAergic)神经元和突触的衰老。了解衰老如何影响特定神经元亚群的突触,可能有助于解释衰老相关效应的异质性。我们回顾了有关衰老对GABA能神经元和突触数量的影响以及它们突触前和突触后成分中与衰老相关变化的文献。最后,我们讨论了这些变化对GABA能系统可塑性的影响,强调了我们关于小鼠体感皮层衰老的研究结果,并将它们与可塑性损伤和脑部疾病联系起来。我们认为,衰老引起的GABA能系统损伤会导致抑制/兴奋失衡,从而降低神经元对环境和细胞挑战做出可塑性变化反应的能力,使大脑更容易受到认知衰退和突触病变疾病损害的影响。